Aristol-9-en-1-ol

Details

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Internal ID 526485d7-50c5-41b5-972a-6eccd4bbc9b9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Aristolane sesquiterpenoids
IUPAC Name (1aR,4S,7R,7aR,7bS)-1,1,7,7a-tetramethyl-2,4,5,6,7,7b-hexahydro-1aH-cyclopropa[a]naphthalen-4-ol
SMILES (Canonical) CC1CCC(C2=CCC3C(C12C)C3(C)C)O
SMILES (Isomeric) C[C@@H]1CC[C@@H](C2=CC[C@@H]3[C@H]([C@@]12C)C3(C)C)O
InChI InChI=1S/C15H24O/c1-9-5-8-12(16)10-6-7-11-13(14(11,2)3)15(9,10)4/h6,9,11-13,16H,5,7-8H2,1-4H3/t9-,11-,12+,13+,15+/m1/s1
InChI Key CSUIUQRZISBPSM-PYISLEMLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Aristol-9-en-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.7959 79.59%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4822 48.22%
OATP2B1 inhibitior - 0.8481 84.81%
OATP1B1 inhibitior + 0.9431 94.31%
OATP1B3 inhibitior + 0.9629 96.29%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9606 96.06%
P-glycoprotein inhibitior - 0.9202 92.02%
P-glycoprotein substrate - 0.8391 83.91%
CYP3A4 substrate + 0.5229 52.29%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.9007 90.07%
CYP2C9 inhibition - 0.6808 68.08%
CYP2C19 inhibition - 0.6260 62.60%
CYP2D6 inhibition - 0.9131 91.31%
CYP1A2 inhibition - 0.7271 72.71%
CYP2C8 inhibition - 0.8050 80.50%
CYP inhibitory promiscuity - 0.7527 75.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5804 58.04%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.7985 79.85%
Skin irritation + 0.5942 59.42%
Skin corrosion - 0.9224 92.24%
Ames mutagenesis - 0.7598 75.98%
Human Ether-a-go-go-Related Gene inhibition - 0.5162 51.62%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5041 50.41%
skin sensitisation + 0.5718 57.18%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6520 65.20%
Acute Oral Toxicity (c) III 0.7919 79.19%
Estrogen receptor binding - 0.6149 61.49%
Androgen receptor binding - 0.5874 58.74%
Thyroid receptor binding - 0.5903 59.03%
Glucocorticoid receptor binding - 0.5911 59.11%
Aromatase binding - 0.6528 65.28%
PPAR gamma - 0.7600 76.00%
Honey bee toxicity - 0.9097 90.97%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity + 0.9726 97.26%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.76% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.22% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.69% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.52% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 85.04% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.89% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.59% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.63% 95.56%
CHEMBL1871 P10275 Androgen Receptor 80.30% 96.43%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Humulus scandens
Kopsia flavida
Ribes sanguineum
Stachys chinensis

Cross-Links

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PubChem 21159118
NPASS NPC49158